Loading…

Synthesis of Tricyclic Diesters from 8-Acetoxytricyclodec-3-ene Monoester

Tricyclic diesters were synthesized in yields of 70.4–90.8% by the addition of С 2 –С 5 monobasic carboxylic acids to tricyclo[5.2.1.0 2,6 ]dec-3-еn-8-yl acetate in the presence of a BF 3 ·OEt 2 catalyst. One of the synthesized diesters, tricyclodec-3,8-diyl diacetate, has a pleasant smell with a ci...

Full description

Saved in:
Bibliographic Details
Published in:Russian journal of general chemistry 2018-03, Vol.88 (3), p.393-396
Main Authors: Mamedov, M. K., Makhmudova, E. G., Rasulova, R. A., Abdullaeva, A. Dzh
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 396
container_issue 3
container_start_page 393
container_title Russian journal of general chemistry
container_volume 88
creator Mamedov, M. K.
Makhmudova, E. G.
Rasulova, R. A.
Abdullaeva, A. Dzh
description Tricyclic diesters were synthesized in yields of 70.4–90.8% by the addition of С 2 –С 5 monobasic carboxylic acids to tricyclo[5.2.1.0 2,6 ]dec-3-еn-8-yl acetate in the presence of a BF 3 ·OEt 2 catalyst. One of the synthesized diesters, tricyclodec-3,8-diyl diacetate, has a pleasant smell with a citrus scent and can be used in different perfume compositions as a flavoring.
doi_str_mv 10.1134/S1070363218030039
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2026485883</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A726584635</galeid><sourcerecordid>A726584635</sourcerecordid><originalsourceid>FETCH-LOGICAL-c307t-5a40e9f96891b22840be69012e7d2f1ff88102b98b833469b209ed8d1fff5ca63</originalsourceid><addsrcrecordid>eNp1kE1PwzAMhiMEEmPwA7hV4hxwkjZLjtP4mjTEYeNctakzMm3NSDqJ_nsyisQBIR9s-X0f2zIh1wxuGRP53ZLBBIQUnCkQAEKfkBGToKgQBZymOsn0qJ-Tixg3AAxA8hGZL_u2e8foYuZttgrO9GbrTHbvMHYYYmaD32WKTg12_rPvBoNv0FBBscXsxbf-23pJzmy1jXj1k8fk7fFhNXumi9en-Wy6oEbApKNFlQNqq6XSrOZc5VCj1MA4ThpumbVKMeC1VrUSIpe65qCxUU1SbGEqKcbkZpi7D_7jkFaXG38IbVpZcuAyV4VK5JjcDq51tcXStdZ3oTIpGtw541u0LvWnEy4LlUtRJIANgAk-xoC23Ae3q0JfMiiPLy7_vDgxfGBi8rZrDL-n_A99AYaze7U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2026485883</pqid></control><display><type>article</type><title>Synthesis of Tricyclic Diesters from 8-Acetoxytricyclodec-3-ene Monoester</title><source>Springer Nature</source><creator>Mamedov, M. K. ; Makhmudova, E. G. ; Rasulova, R. A. ; Abdullaeva, A. Dzh</creator><creatorcontrib>Mamedov, M. K. ; Makhmudova, E. G. ; Rasulova, R. A. ; Abdullaeva, A. Dzh</creatorcontrib><description>Tricyclic diesters were synthesized in yields of 70.4–90.8% by the addition of С 2 –С 5 monobasic carboxylic acids to tricyclo[5.2.1.0 2,6 ]dec-3-еn-8-yl acetate in the presence of a BF 3 ·OEt 2 catalyst. One of the synthesized diesters, tricyclodec-3,8-diyl diacetate, has a pleasant smell with a citrus scent and can be used in different perfume compositions as a flavoring.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363218030039</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Acetic acid ; Carboxylic acids ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Dicyclopentadiene ; Diesters ; Organic compounds ; Smell</subject><ispartof>Russian journal of general chemistry, 2018-03, Vol.88 (3), p.393-396</ispartof><rights>Pleiades Publishing, Ltd. 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Copyright Springer Science &amp; Business Media 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Mamedov, M. K.</creatorcontrib><creatorcontrib>Makhmudova, E. G.</creatorcontrib><creatorcontrib>Rasulova, R. A.</creatorcontrib><creatorcontrib>Abdullaeva, A. Dzh</creatorcontrib><title>Synthesis of Tricyclic Diesters from 8-Acetoxytricyclodec-3-ene Monoester</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>Tricyclic diesters were synthesized in yields of 70.4–90.8% by the addition of С 2 –С 5 monobasic carboxylic acids to tricyclo[5.2.1.0 2,6 ]dec-3-еn-8-yl acetate in the presence of a BF 3 ·OEt 2 catalyst. One of the synthesized diesters, tricyclodec-3,8-diyl diacetate, has a pleasant smell with a citrus scent and can be used in different perfume compositions as a flavoring.</description><subject>Acetic acid</subject><subject>Carboxylic acids</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Dicyclopentadiene</subject><subject>Diesters</subject><subject>Organic compounds</subject><subject>Smell</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PwzAMhiMEEmPwA7hV4hxwkjZLjtP4mjTEYeNctakzMm3NSDqJ_nsyisQBIR9s-X0f2zIh1wxuGRP53ZLBBIQUnCkQAEKfkBGToKgQBZymOsn0qJ-Tixg3AAxA8hGZL_u2e8foYuZttgrO9GbrTHbvMHYYYmaD32WKTg12_rPvBoNv0FBBscXsxbf-23pJzmy1jXj1k8fk7fFhNXumi9en-Wy6oEbApKNFlQNqq6XSrOZc5VCj1MA4ThpumbVKMeC1VrUSIpe65qCxUU1SbGEqKcbkZpi7D_7jkFaXG38IbVpZcuAyV4VK5JjcDq51tcXStdZ3oTIpGtw541u0LvWnEy4LlUtRJIANgAk-xoC23Ae3q0JfMiiPLy7_vDgxfGBi8rZrDL-n_A99AYaze7U</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Mamedov, M. K.</creator><creator>Makhmudova, E. G.</creator><creator>Rasulova, R. A.</creator><creator>Abdullaeva, A. Dzh</creator><general>Pleiades Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20180301</creationdate><title>Synthesis of Tricyclic Diesters from 8-Acetoxytricyclodec-3-ene Monoester</title><author>Mamedov, M. K. ; Makhmudova, E. G. ; Rasulova, R. A. ; Abdullaeva, A. Dzh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-5a40e9f96891b22840be69012e7d2f1ff88102b98b833469b209ed8d1fff5ca63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetic acid</topic><topic>Carboxylic acids</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Dicyclopentadiene</topic><topic>Diesters</topic><topic>Organic compounds</topic><topic>Smell</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mamedov, M. K.</creatorcontrib><creatorcontrib>Makhmudova, E. G.</creatorcontrib><creatorcontrib>Rasulova, R. A.</creatorcontrib><creatorcontrib>Abdullaeva, A. Dzh</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mamedov, M. K.</au><au>Makhmudova, E. G.</au><au>Rasulova, R. A.</au><au>Abdullaeva, A. Dzh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Tricyclic Diesters from 8-Acetoxytricyclodec-3-ene Monoester</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2018-03-01</date><risdate>2018</risdate><volume>88</volume><issue>3</issue><spage>393</spage><epage>396</epage><pages>393-396</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>Tricyclic diesters were synthesized in yields of 70.4–90.8% by the addition of С 2 –С 5 monobasic carboxylic acids to tricyclo[5.2.1.0 2,6 ]dec-3-еn-8-yl acetate in the presence of a BF 3 ·OEt 2 catalyst. One of the synthesized diesters, tricyclodec-3,8-diyl diacetate, has a pleasant smell with a citrus scent and can be used in different perfume compositions as a flavoring.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363218030039</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1070-3632
ispartof Russian journal of general chemistry, 2018-03, Vol.88 (3), p.393-396
issn 1070-3632
1608-3350
language eng
recordid cdi_proquest_journals_2026485883
source Springer Nature
subjects Acetic acid
Carboxylic acids
Chemical synthesis
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Dicyclopentadiene
Diesters
Organic compounds
Smell
title Synthesis of Tricyclic Diesters from 8-Acetoxytricyclodec-3-ene Monoester
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T18%3A15%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20Tricyclic%20Diesters%20from%208-Acetoxytricyclodec-3-ene%20Monoester&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Mamedov,%20M.%20K.&rft.date=2018-03-01&rft.volume=88&rft.issue=3&rft.spage=393&rft.epage=396&rft.pages=393-396&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363218030039&rft_dat=%3Cgale_proqu%3EA726584635%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c307t-5a40e9f96891b22840be69012e7d2f1ff88102b98b833469b209ed8d1fff5ca63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2026485883&rft_id=info:pmid/&rft_galeid=A726584635&rfr_iscdi=true